The T99K variant of glycosylasparaginase shows a new structural mechanism of the genetic disease aspartylglucosaminuria

Author:

Pande Suchita1,Guo Hwai‐Chen1ORCID

Affiliation:

1. Department of Biological SciencesUniversity of Massachusetts Lowell Lowell Massachusetts, 01854

Funder

National Institutes of Health

Publisher

Wiley

Subject

Molecular Biology,Biochemistry

Reference39 articles.

1. Systematic use of the incomplete factorial approach in the design of protein crystallization experiments;Abergel C;J Biol Chem,1991

2. Aspartylglycosaminuria: An inborn error of glycoprotein catabolism

3. Aspartylglycosaminuria: a review

4. Aspartylglycosaminuria (agu). Further aspects on its clinical picture, mode of inheritance and epidemiology based on a series of 57 patients;Autio S;Ann Clin Res,1973

5. Aspartylglycosaminuria: biochemistry and molecular biology

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Aspartylglucosaminuria: Clinical Presentation and Potential Therapies;Journal of Child Neurology;2021-01-13

2. Disorders of glycoprotein degradation: sialidosis, fucosidosis, α-mannosidosis, β-mannosidosis, and aspartylglycosaminuria;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020

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